US3432458A - Thickened polymerizable unsaturated polyester resin compositions and fibrous substances impregnated therewith - Google Patents

Thickened polymerizable unsaturated polyester resin compositions and fibrous substances impregnated therewith Download PDF

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US3432458A
US3432458A US677246A US3432458DA US3432458A US 3432458 A US3432458 A US 3432458A US 677246 A US677246 A US 677246A US 3432458D A US3432458D A US 3432458DA US 3432458 A US3432458 A US 3432458A
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polyester resin
unsaturated polyester
thickened
weight
glycol
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Fred K C Kwan
Richard C Ross
Glenn R Svoboda
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Freeman Chemical Corp
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/05Alcohols; Metal alcoholates
    • C08K5/053Polyhydroxylic alcohols

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  • This invention relates to polymerizable resinous compositions in which fibrous reinforcing substances such as glass fibers are impregnated with polymerizable resinous compositions to produce a dried, hardened, impregnated fibrous composition which can be heated and will flow prior to curing.
  • the compositions are curable to produce thermoset plastic substances.
  • Glass fiber reinforced polyester resin products are well known in the art. They comprise chopped glass fibers, woven glass tfiber fabrics and randomly oriented glass fiber mats as reinforcement for a cured thermoset mass of unsaturated polyester resin. Customarily the polyester resin is applied as a liquid spray or dip to the fibrous reinforcing material immediately prior to the curing of the resin. See 3,243,949; 2,927,623. It is however known to apply a liquid state unsaturated polyester resin composition to fibrous reinforcing materials and to thicken the liquid polyester resin without causing significant gelation and curing thereof. See, for example, US. Patent 2,628,209 wherein a small quantity of magnesium oxide is included With the unsaturated polyester resin composition to cause it to become thickened without significant gelation when applied as an impregnant for the fibrous reinforcing substances.
  • the thickened resin is essentially dry to the touch and the impregnated fibers can be transported conveniently for subsequent use in the preparation of thermoset reinforced plastic articles.
  • Calcium oxide has been described as incapable of thickening unsaturated polyester resins. See U.S. Patent 2,628,209 supra. Calcium oxide is described elsewhere as accelerating the conjoint polymerization of unsaturated polyesters and styrene. See US. Patent 2,568,331. For the purposes of the present application, it is essential that the resinous composition be merely thickened without significant accompanying polymerization.
  • Unsaturated polyester resin compositions are blended with from 0.5 to 4.0 parts by weight (based on parts of the resin) of a polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine. That mixture is blended With 0.5 to 10.0 parts by Weight of an alkaline earth oxide which can be calcium oxide or magnesium oxide. The resulting mixture remains fluid for a sufficiently long period of time to permit impregnation 0f fibrous reinforcing materials and thereafter, without curing, becomes thickened and substantially dry to the touch, yet remains polymerizable.
  • a polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine. That mixture is blended With 0.5 to 10.0 parts by Weight of an alkaline earth oxide which can be calcium oxide or magnesium oxide.
  • the resulting mixture remains fluid for a sufficiently long period of time to permit impregnation 0f
  • the described polyhydric alcohol achieves thickening of the unsaturated polyester resin composition with calcium oxideheretofore considered to be inoperable as a thickening agent.
  • the inclusion of the described polyhydric alcohol hastens the heretofore known thickening which is achieved with a specified amount of magnesium oxide or, alternatively, allows the heretofore known thickening to be accomplished with a smaller amount of magnesium oxide that can be accomplished without the polyhydric alcohol.
  • An unsaturated polyester resin composition can be prepared by polyesterification of a dihydric alcohol such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, butylene glycol, neopentyl glycol and the like with a dicarboxylic acid or dicarboxylic acid anhydride wherein at least a portion of the dicarboxylic acid or anhydride includes alpha-beta-ethylenic unsaturation.
  • a dihydric alcohol such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, butylene glycol, neopentyl glycol and the like
  • a dicarboxylic acid or dicarboxylic acid anhydride wherein at least a portion of the dicarboxylic acid or anhydride includes alpha-beta-ethylenic unsaturation.
  • Typical dicarboxylic materials include phthalic acid, isophthalic acid, phthalic anhydride, terephthalic acid, fumaric acid, maleic acid, maleic anhydride, tetrachlorophthalic acid and anhydride, itaconic acid, citraconic acid and the like.
  • a copolymerizable monomer having terminal (bCH grouping, is included with the polyester, e.g., styrene, chloro-styrene, methyl styrene, acrylic acid, methacrylic acid, alkyl acrylates and methacrylates, divinyl benzene, diallyl phthalate, and the like.
  • the unsaturated polyester resin compositions customarily contain an inhibitor of vinyl polymerization such as hydroquinone, toluhydroquinone, tert-butyl catechol for example.
  • the composition also contains a quantity, preferably from about 0.5 to 2.0 percent by weight, of a high temperature curing catalyst for the resin.
  • the catalyst is one which will not initiate the polymerization at the liquid-state temperatures at which the composition is applied to the fibrous materials.
  • the catalyst also is preferably one whose decomposition is not induced by metal-ions.
  • the unsaturated polyester resin composition also may contain thixotropic agents such as aerated silica aerogel.
  • polyester resin compositions are well known, e.g., Polyesters and their Applications, Bjorksten et al., Reinhold, 1960.
  • preferred catalysts are dicumyl peroxide, tert-butyl peroxide and tert-butyl perbenzoate.
  • An unsaturated polyester resin also may be prepared by the polyesterification of a polyepoxide such as diglycidyl ether of Bisphenol-A With acrylic or methacrylic acid.
  • a polyepoxide such as diglycidyl ether of Bisphenol-A With acrylic or methacrylic acid.
  • Such products include plural ester linkages and plural alpha-beta ethylenic unsaturation and are essentially free of unreacted epoxy groups.
  • the unsaturated polyester resin composition is combined with 0.5 to 4.0 percent by weight and preferably about 2% by weight of polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine. Thereafter the mixture is combined with 0.5 to 10.0 parts by weight of alkaline earth oxide which can be calcium oxide or magnesium oxide.
  • alkaline earth oxide may be partially hydrolyzed to include a minor quantity of the alkaline earth hydroxide. However, excess hydroxyl content prevents the desired thickening from occurring.
  • Example I An unsaturated polyester resin was prepared from 1.09 mols propylene glycol, 0.60 mols phthalic anhydride, 0.40 mols maleic anhydride. The reactants were heated in a reaction kettle for several hours until a low acid number indicated substantially complete reaction. The unreacted propylene glycol was stripped from the system and the resin was cut back with 29 parts by weight styrene. As a polymerization inhibitor, 0.01 weight percent hydroquinone was added.
  • the polyester resin had an initial viscosity of 2500 centipoises.
  • the thickened polyester resin compositions could be heated and caused to flow without concurrent gelation and hardening. By the addition of substantial heat, the resinous compositions could be cured to a hardened thermoset condition.
  • polyhydric materials isopropyl alcohol, propylene glycol, dipropylene glycol, polypropylene glycol-425, ethylene glycol, diethylene glycol, polyethylene glycol-600, glycerine, trimethylolpropane, pentaerythritol and sorbitol.
  • Polypropylene glycol-425 is a mixture of polypropylene glycols having an average molecular weight of 425.
  • polyethylene glycol-600 is a mixture of polyethylene glycols having an average molecular weight of 600.
  • the described unsaturated polyester resin Composition I was combined with 5% by weight calcium oxide and 2% by weight of the polyhydric alcohol.
  • the viscosity of the composition was measured at the end of 2 hours and at the end of 24 hours.
  • the viscosities of the mixtures are set forth in the following table.
  • Similar thickening can be achieved with magnesium oxide in place of the calcium oxide when the polyhydric alcohol is included in accordance with this invention.
  • the thickening achieved with magnesium oxide is brought about in less time or is achieved with less magnesium oxide than the thickening which is obtained with magnesium alone in accordance with the prior art, i.e., U.S. Patent 2,628,209.
  • Glass fiber roving comprising multi-strand glass fibers, can be impregnated with the present unsaturated polyester resin compositions while they are in their relatively fluid state. Thereafter the roving can be coiled or spooled and the resin composition allowed to thicken.
  • a preferred embodiment of the present invention involves the impregnation of a spooled mat of randomly oriented glass fibers of the general type described in US. Patent 3,276,- 928.
  • the impregnated mat while still relatively moist, is recoiled with a barrier membrane such as cellophane or polyethylene sheeting between the wraps of the spool.
  • the polyester resin thickens and hardens without gelation when the present compositions are employed as the impregnant.
  • Woven glass fiber fabrics also are useful as the reinforcing material which is coated with the thickened polymerizable compositions.
  • the liquid state composition which is applied as a coating to the fibrous materials contains all of the ingredients to keep the coated fibrous material intact for commercially feasible storage periods and to cause the resinous constituents to cure when heated above the liquid state coating temperature.
  • the coated fibrous material is merely introduced into a heated mold whence it flows initially to fill the cavity and conform to the mold. Thereafter the resin polymerizes in the mold cavity and the desired thermoset product is produced.
  • Reinforced unsaturated polyester resin laminates may contain from about to about 60 percent resin and the balance glass reinforcement. Usually the resin content is about to percent with the glass reinforcement comprising the remaining to 50 percent. Accordingly the amount of the resinous composition applied to the fibrous reinforcement should be from about 0.1 to about 1.5 times the fiber weight, and preferably from about 0.33 to 1.0 times the fiber weight.
  • the preferred unsaturated polyester resins contain about 45 to parts by Weight of the polymerizable polyester and from about 55 to 10 parts by weight of copolymerizable monomer.
  • a thickened polymerizable resinous composition essentialy dry to the touch and capable of flowing without curing upon heating, said resinous composition including:
  • polyesterification reaction product of polyhydric alcohol and dicarboxylic material selected from the class consisting of dicarboxylic acids and dicarboxylic acid anhydrides, at least a portion of said dicarboxylic material comprising ethylenically unsaturated dicarboxylic acid or acid anhydride;
  • polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine;
  • (C) from 0.5 to 10.0 parts by weight of alkaline earth oxide selected from the class consisting of calcium oxide and magnesium oxide.
  • fibrous reinforcement of claim 2 wherein the fibrous reinforcing components are Woven glass fiber fabrics.
  • a coiled fibrous reinforcement mat, dry-to-the-touch, comprising a randomly oriented glass fiber mat, coated with the resinous composition of claim 1.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Reinforced Plastic Materials (AREA)

Description

March 11, 1969 F. K. c. KWAN ETAL 3 4 2 THICKENED POLYMERIZABLE UNSATURATED POLYESTER 3 RESIN COMPOSITIONS AND FIBROUS SUBSTANCES IMPREGNATED THEREWITH Filed Oct. 23. 1967 Polymerizable Unsaturated Polyester Resin Composition Including Copolymerizable Monomer, e.g. Styrene Polyhydric Alcohol M I X I N G Alkaline Earth Oxide Liquid state Composition F I B E R Fibrous Reinforcement,
/ c 0 A T I N G e.g. glass fiber mat Moist Fibrous Materials T H I C K E N I N G Resin Composition INVENTORS Fred K. C. Kwan Richard C. Ross Glenn R. Svobo a Attorney United States Patent 3,432,458 THICKENED POLYMERIZABLE UNSATURATED POLYESTER RESIN COMPOSITIONS AND FI- SUBSTANCES IMPREGNATED THERE- Fred K. 'C. Kwan, Chicago, Ill., and Richard C. Ross, Port Washington, and Glenn R. Svoboda, Grafton, Wis., assignors to Freeman Chemical Corporation, Port Washington, Wis., a corporation of Delaware Filed Oct. 23, 1967, Ser. No. 677,246 US. Cl. 26033.4 Int. Cl. C08f 21/02, 45/34, 45/10 7 Claims ABSTRACT OF THE DISCLOSURE BACKGROUND OF THE INVENTION Field of the invention This invention relates to polymerizable resinous compositions in which fibrous reinforcing substances such as glass fibers are impregnated with polymerizable resinous compositions to produce a dried, hardened, impregnated fibrous composition which can be heated and will flow prior to curing. The compositions are curable to produce thermoset plastic substances.
Description of the prior art Glass fiber reinforced polyester resin products are well known in the art. They comprise chopped glass fibers, woven glass tfiber fabrics and randomly oriented glass fiber mats as reinforcement for a cured thermoset mass of unsaturated polyester resin. Customarily the polyester resin is applied as a liquid spray or dip to the fibrous reinforcing material immediately prior to the curing of the resin. See 3,243,949; 2,927,623. It is however known to apply a liquid state unsaturated polyester resin composition to fibrous reinforcing materials and to thicken the liquid polyester resin without causing significant gelation and curing thereof. See, for example, US. Patent 2,628,209 wherein a small quantity of magnesium oxide is included With the unsaturated polyester resin composition to cause it to become thickened without significant gelation when applied as an impregnant for the fibrous reinforcing substances.
The thickened resin is essentially dry to the touch and the impregnated fibers can be transported conveniently for subsequent use in the preparation of thermoset reinforced plastic articles.
Calcium oxide has been described as incapable of thickening unsaturated polyester resins. See U.S. Patent 2,628,209 supra. Calcium oxide is described elsewhere as accelerating the conjoint polymerization of unsaturated polyesters and styrene. See US. Patent 2,568,331. For the purposes of the present application, it is essential that the resinous composition be merely thickened without significant accompanying polymerization.
Summary of the invention Unsaturated polyester resin compositions are blended with from 0.5 to 4.0 parts by weight (based on parts of the resin) of a polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine. That mixture is blended With 0.5 to 10.0 parts by Weight of an alkaline earth oxide which can be calcium oxide or magnesium oxide. The resulting mixture remains fluid for a sufficiently long period of time to permit impregnation 0f fibrous reinforcing materials and thereafter, without curing, becomes thickened and substantially dry to the touch, yet remains polymerizable. The described polyhydric alcohol achieves thickening of the unsaturated polyester resin composition with calcium oxideheretofore considered to be inoperable as a thickening agent. The inclusion of the described polyhydric alcohol hastens the heretofore known thickening which is achieved with a specified amount of magnesium oxide or, alternatively, allows the heretofore known thickening to be accomplished with a smaller amount of magnesium oxide that can be accomplished without the polyhydric alcohol.
Brief description of the drawings The single drawing is a schematic flow diagram illustrating the present invention.
Description of the preferred embodiment An unsaturated polyester resin composition can be prepared by polyesterification of a dihydric alcohol such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, butylene glycol, neopentyl glycol and the like with a dicarboxylic acid or dicarboxylic acid anhydride wherein at least a portion of the dicarboxylic acid or anhydride includes alpha-beta-ethylenic unsaturation. Typical dicarboxylic materials include phthalic acid, isophthalic acid, phthalic anhydride, terephthalic acid, fumaric acid, maleic acid, maleic anhydride, tetrachlorophthalic acid and anhydride, itaconic acid, citraconic acid and the like. A copolymerizable monomer having terminal (bCH grouping, is included with the polyester, e.g., styrene, chloro-styrene, methyl styrene, acrylic acid, methacrylic acid, alkyl acrylates and methacrylates, divinyl benzene, diallyl phthalate, and the like. The unsaturated polyester resin compositions customarily contain an inhibitor of vinyl polymerization such as hydroquinone, toluhydroquinone, tert-butyl catechol for example. The composition also contains a quantity, preferably from about 0.5 to 2.0 percent by weight, of a high temperature curing catalyst for the resin. The catalyst is one which will not initiate the polymerization at the liquid-state temperatures at which the composition is applied to the fibrous materials. The catalyst also is preferably one whose decomposition is not induced by metal-ions. The unsaturated polyester resin composition also may contain thixotropic agents such as aerated silica aerogel. The proportion and use of unsaturated polyester resin compositions is well known, e.g., Polyesters and their Applications, Bjorksten et al., Reinhold, 1960. Examples of preferred catalysts are dicumyl peroxide, tert-butyl peroxide and tert-butyl perbenzoate.
An unsaturated polyester resin also may be prepared by the polyesterification of a polyepoxide such as diglycidyl ether of Bisphenol-A With acrylic or methacrylic acid. Such products include plural ester linkages and plural alpha-beta ethylenic unsaturation and are essentially free of unreacted epoxy groups. These polyesters are described, for example, in British patents 1,006,587 and 1,030,760.
Free polyhydric alcohol The unsaturated polyester resin composition is combined with 0.5 to 4.0 percent by weight and preferably about 2% by weight of polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine. Thereafter the mixture is combined with 0.5 to 10.0 parts by weight of alkaline earth oxide which can be calcium oxide or magnesium oxide. The alkaline earth oxide may be partially hydrolyzed to include a minor quantity of the alkaline earth hydroxide. However, excess hydroxyl content prevents the desired thickening from occurring.
Example I An unsaturated polyester resin was prepared from 1.09 mols propylene glycol, 0.60 mols phthalic anhydride, 0.40 mols maleic anhydride. The reactants were heated in a reaction kettle for several hours until a low acid number indicated substantially complete reaction. The unreacted propylene glycol was stripped from the system and the resin was cut back with 29 parts by weight styrene. As a polymerization inhibitor, 0.01 weight percent hydroquinone was added.
The polyester resin had an initial viscosity of 2500 centipoises.
Five parts by weight of calcium oxide was added to 100 parts by weight of the resin and the viscosity of the mixture was measured over a period of 4 days as set forth in the following table:
Table I--Viscosity of resin, Example I Time, hours: Viscosity, poises tive. Resin Composition II was mixed with 1% by weight propylene glycol, 2% by weight propylene glycol and 5% by weight of calcium oxide was added and the viscosity was measured through 24 hours. The viscosity values are set forth in the following table.
TABLE II.-VISCOSITY OF COMPOSITIONS OF UNSA'IU RATED POLYESTER AND 5% BY WEIGHT CALCIUM OXIDE, POISES Free propylene glycol content Clear resin I Filled resin II Time, hours 1% 2% 5% 1% 2% 5% From the foregoing table it can be seen that the combination of propylene glycol and 5% by weight calcium oxide increases the viscosity of the unsaturated polyester resin composition above 1000 poises (except in the instance of the 5% resin dilution where a substantial increase in viscosity was nonetheless observed).
In all instances the thickened polyester resin compositions could be heated and caused to flow without concurrent gelation and hardening. By the addition of substantial heat, the resinous compositions could be cured to a hardened thermoset condition.
In an effort to show the unique character of the selected polyhydric alcohols for the present purposes, a series of comparative tests was conducted with the following polyhydric materials: isopropyl alcohol, propylene glycol, dipropylene glycol, polypropylene glycol-425, ethylene glycol, diethylene glycol, polyethylene glycol-600, glycerine, trimethylolpropane, pentaerythritol and sorbitol. Note: Polypropylene glycol-425 is a mixture of polypropylene glycols having an average molecular weight of 425. Similarly polyethylene glycol-600 is a mixture of polyethylene glycols having an average molecular weight of 600. In each instance the described unsaturated polyester resin Composition I was combined with 5% by weight calcium oxide and 2% by weight of the polyhydric alcohol. The viscosity of the composition was measured at the end of 2 hours and at the end of 24 hours. The viscosities of the mixtures are set forth in the following table.
TABLE III.VISCOSITIES OF UNSA'IURATED POLYESTER RESIN COMPOSITIONS Afterlolyhydric additive Initial 2 hours 24 hours lsopropyl alcohol 14 14 21 Propylene glycol 10. 5 20 1, 000 Dipropylene glyeol 15.2 24 1, 000 Polypropylene glycol-425. 16 25 36 Ethylene glycol 20 45 1, 000 Diethylene glycol 20 1,000 Polyethylene glycol600 20 20 30 Glyeeriue 22. 5 1, 000 Trimethylcl propane 13.4 23 Pentraerytlu'itol 14. 0 25 29 Sorbitol 13 28 35 No additive 1&1 22 29 From inspection of the foregoing table it will be seen that the propylene glycol, dipropylene glycol, ethylene glycol, diethylene glycol and glycerine uniquely achieve the desired viscosity increase in the unsaturated polyester resin composition in combination with calcium oxide.
Similar thickening can be achieved with magnesium oxide in place of the calcium oxide when the polyhydric alcohol is included in accordance with this invention. The thickening achieved with magnesium oxide is brought about in less time or is achieved with less magnesium oxide than the thickening which is obtained with magnesium alone in accordance with the prior art, i.e., U.S. Patent 2,628,209.
Glass fiber roving comprising multi-strand glass fibers, can be impregnated with the present unsaturated polyester resin compositions while they are in their relatively fluid state. Thereafter the roving can be coiled or spooled and the resin composition allowed to thicken. A preferred embodiment of the present invention involves the impregnation of a spooled mat of randomly oriented glass fibers of the general type described in US. Patent 3,276,- 928. The impregnated mat, while still relatively moist, is recoiled with a barrier membrane such as cellophane or polyethylene sheeting between the wraps of the spool. The polyester resin thickens and hardens without gelation when the present compositions are employed as the impregnant. Woven glass fiber fabrics also are useful as the reinforcing material which is coated with the thickened polymerizable compositions.
The accompanying drawing illustrates schematically the starting materials and the processing steps of the preferred embodiment of the invention. The liquid state composition which is applied as a coating to the fibrous materials contains all of the ingredients to keep the coated fibrous material intact for commercially feasible storage periods and to cause the resinous constituents to cure when heated above the liquid state coating temperature. The coated fibrous material is merely introduced into a heated mold whence it flows initially to fill the cavity and conform to the mold. Thereafter the resin polymerizes in the mold cavity and the desired thermoset product is produced.
Reinforced unsaturated polyester resin laminates may contain from about to about 60 percent resin and the balance glass reinforcement. Usually the resin content is about to percent with the glass reinforcement comprising the remaining to 50 percent. Accordingly the amount of the resinous composition applied to the fibrous reinforcement should be from about 0.1 to about 1.5 times the fiber weight, and preferably from about 0.33 to 1.0 times the fiber weight.
The preferred unsaturated polyester resins contain about 45 to parts by Weight of the polymerizable polyester and from about 55 to 10 parts by weight of copolymerizable monomer.
We claim:
1. A thickened polymerizable resinous composition, essentialy dry to the touch and capable of flowing without curing upon heating, said resinous composition including:
(A) parts by weight of polymerizable polyester resin comprising from 10 to 55 parts by weight of a copolymerizable monomer containing a terminal C=CH group and 90 to 45 parts by wei ht of an unsaturated polyester selected from the class con sisting of:
(a) the polyesterification reaction product of polyhydric alcohol and dicarboxylic material selected from the class consisting of dicarboxylic acids and dicarboxylic acid anhydrides, at least a portion of said dicarboxylic material comprising ethylenically unsaturated dicarboxylic acid or acid anhydride; and
(b) the polyesterification reaction product of a polyepoxide and ethylenically unsaturated monocarboxylic acid;
(B) from 0.5 to 4.0 parts by weight of polyhydric alcohol selected from the class consisting of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol and glycerine;
(C) from 0.5 to 10.0 parts by weight of alkaline earth oxide selected from the class consisting of calcium oxide and magnesium oxide.
2. A fibrous reinforcement, dry-to-the-touch, including fibrous reinforcing components which are coated with an unpolymerized polymerizable resinous composition of claim 1.
3. The fibrous reinforcement of claim 2 wherein the fibrous reinforcing components are randomly oriented glass fibers.
4. The fibrous reinforcement of claim 2 wherein the fibrous reinforcing components are Woven glass fiber fabrics.
5. A coiled fibrous reinforcement mat, dry-to-the-touch, comprising a randomly oriented glass fiber mat, coated with the resinous composition of claim 1.
6. The method of preparing a dry-to-the-touch fibrous reinforcement impregnated with suflicient unpolymerized polymerizable unsaturated polyester resinous composition of claim 1 which comprises heating the said resinous composition to a liquid state impregnating the fibrous mat with the liquid state References Cited UNITED STATES PATENTS 2 ,628,209 2/1953 Fisk 26086l X 3,131,148 4/1964 Taulli 260-40 X 3,338,850 8/1967 Sbarra et a1 26040 X MORRIS LIEBMAN, Primary Examiner.
L. T. JACOBS, Assistant Examiner.
US. Cl. XR 260--40, 861, 863
US677246A 1967-10-23 1967-10-23 Thickened polymerizable unsaturated polyester resin compositions and fibrous substances impregnated therewith Expired - Lifetime US3432458A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3668178A (en) * 1969-04-01 1972-06-06 Union Carbide Corp Unsaturated polyester resins admixed with cyclic ester polymers
DE2311395A1 (en) * 1973-03-08 1974-09-12 Basf Ag Process for the production of hardenable polyester molding compounds
US3922247A (en) * 1973-06-15 1975-11-25 Gulf Research Development Co Handleable, moldable ester-type resin compositions
USRE30583E (en) * 1979-01-24 1981-04-21 The Dow Chemical Company Vinyl ester resin compositions containing dicyclopentadiene alkenoate
US4355123A (en) * 1980-12-16 1982-10-19 General Electric Company Cured polyester compositions and process for their production
US4472544A (en) * 1982-07-27 1984-09-18 Cdf-Chimie S.A. Anti-shrink additive for unsaturated polyester, its fabrication process, and anti-shrink compositions
US4581393A (en) * 1983-02-22 1986-04-08 The Dow Chemical Company Glass fiber reinforced vinylized epoxy compositions with reduced fiber prominence
US5393808A (en) * 1987-10-16 1995-02-28 The Swan Corporation Composition of matter for wear surfaces and method for producing same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4197390A (en) * 1979-02-22 1980-04-08 Shell Oil Company Thickenable thermosetting vinyl ester resins

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2628209A (en) * 1947-10-28 1953-02-10 Us Rubber Co Process for increasing viscosity of uncured alkyd copolymer resinous mixtures and product
US3131148A (en) * 1961-01-13 1964-04-28 Monsanto Chemicals Thickened compositions
US3338850A (en) * 1965-05-06 1967-08-29 Ibm Fumaric acid-rosin adduct/polyester varnish moisture-set ink vehicle and ink compositions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2628209A (en) * 1947-10-28 1953-02-10 Us Rubber Co Process for increasing viscosity of uncured alkyd copolymer resinous mixtures and product
US3131148A (en) * 1961-01-13 1964-04-28 Monsanto Chemicals Thickened compositions
US3338850A (en) * 1965-05-06 1967-08-29 Ibm Fumaric acid-rosin adduct/polyester varnish moisture-set ink vehicle and ink compositions

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3668178A (en) * 1969-04-01 1972-06-06 Union Carbide Corp Unsaturated polyester resins admixed with cyclic ester polymers
DE2311395A1 (en) * 1973-03-08 1974-09-12 Basf Ag Process for the production of hardenable polyester molding compounds
US3922247A (en) * 1973-06-15 1975-11-25 Gulf Research Development Co Handleable, moldable ester-type resin compositions
USRE30583E (en) * 1979-01-24 1981-04-21 The Dow Chemical Company Vinyl ester resin compositions containing dicyclopentadiene alkenoate
US4355123A (en) * 1980-12-16 1982-10-19 General Electric Company Cured polyester compositions and process for their production
US4472544A (en) * 1982-07-27 1984-09-18 Cdf-Chimie S.A. Anti-shrink additive for unsaturated polyester, its fabrication process, and anti-shrink compositions
US4581393A (en) * 1983-02-22 1986-04-08 The Dow Chemical Company Glass fiber reinforced vinylized epoxy compositions with reduced fiber prominence
US5393808A (en) * 1987-10-16 1995-02-28 The Swan Corporation Composition of matter for wear surfaces and method for producing same

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